Imaging and fluid biomarkers in frontotemporal dementia

被引:0
|
作者
Lieke H. Meeter
Laura Donker Kaat
Jonathan D. Rohrer
John C. van Swieten
机构
[1] Erasmus Medical Center,Department of Neurology
[2] Leiden University Medical Center,Department of Clinical Genetics
[3] Dementia Research Centre,Department of Neurodegenerative diseases
[4] Institute of Neurology,Department of Clinical Genetics
[5] Queen Square,undefined
[6] University College London,undefined
[7] VU University Medical Center,undefined
来源
Nature Reviews Neurology | 2017年 / 13卷
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摘要
Most of the validated biomarkers in frontotemporal dementia (FTD) are used to differentiate patients with FTD from patients with Alzheimer disease or from control individualsCurrently validated biomarkers in FTD include grey matter atrophy, alterations in brain metabolism as detected by 18F-fluorodeoxyglucose-PET and cerebrospinal fluid levels of amyloid-β1–42, phospho-tau181 and total-tau.New imaging biomarkers, detected via techniques such as arterial spin labelling and diffusion tensor imaging, are sensitive to the subtle changes that precede grey matter atrophy in FTD, potentially enabling use in diagnosis and disease monitoringPromising fluid biomarkers include neurofilament light chain (for staging, monitoring and prognosis in all FTD subtypes) and dipeptide-repeat proteins and progranulin (for target engagement in gene-specific forms of FTD)Reliable biomarkers that differentiate between tau pathology and TDP-43 pathology are still needed, to facilitate trials of disease-modifying treatmentsFuture research should focus on the multimodal combination of fluid and imaging biomarkers, as well as the harmonization of biomarker collection and analysis protocols
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页码:406 / 419
页数:13
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